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Jasmine extract helps skin cell growth and makes artificial skin thicker, especially when used with skin-derived precursors.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

Rice bran extract caused moderate skin irritation but no eye irritation, while a diluted essence was not irritating to skin and only slightly to guinea pigs.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

Hair follicle stem cells prevent melanocyte stem cells from differentiating by controlling retinoic acid levels.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

KFSD is a rare condition causing scarring hair loss, with no effective treatment known at the time of the report.

T cell subsets are crucial in kidney cancer, and a new model predicts patient outcomes using key genes.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

The gene Prss53 affects hair shape and bone development in rabbits.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

Deleting the scd1 gene in mice prevents obesity by disrupting skin lipids and improving heat regulation.

UTX is important for skin health and its loss can lead to skin issues, especially in females.

Sweat gland stem cells help maintain glands, aid wound healing, and can regenerate skin structures.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Lhx2 helps retinal cells respond to signals for eye development.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Rezpegaldesleukin shows promise for treating severe alopecia areata.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

Msx2 is essential for proper enamel formation by preventing abnormal cell transformation.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Low-penetration genes might help personalize colorectal cancer prevention.